CN108403473B - A composition used as cosmetic - Google Patents
A composition used as cosmetic Download PDFInfo
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- CN108403473B CN108403473B CN201711002041.4A CN201711002041A CN108403473B CN 108403473 B CN108403473 B CN 108403473B CN 201711002041 A CN201711002041 A CN 201711002041A CN 108403473 B CN108403473 B CN 108403473B
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- silicone oil
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- viscosity silicone
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- 239000000203 mixture Substances 0.000 title claims abstract description 46
- 239000002537 cosmetic Substances 0.000 title claims abstract description 19
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 84
- 229920002545 silicone oil Polymers 0.000 claims abstract description 45
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229930003268 Vitamin C Natural products 0.000 claims abstract description 42
- 235000019154 vitamin C Nutrition 0.000 claims abstract description 42
- 239000011718 vitamin C Substances 0.000 claims abstract description 42
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 24
- 239000003995 emulsifying agent Substances 0.000 claims description 17
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 16
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 16
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 16
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 16
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052710 silicon Inorganic materials 0.000 claims description 12
- 239000010703 silicon Substances 0.000 claims description 12
- -1 polydimethylsiloxane Polymers 0.000 claims description 11
- 239000002994 raw material Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 230000002087 whitening effect Effects 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 8
- 229940008099 dimethicone Drugs 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 5
- 229920006037 cross link polymer Polymers 0.000 claims description 4
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims description 3
- 229940086555 cyclomethicone Drugs 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 abstract description 5
- 239000012071 phase Substances 0.000 description 30
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 20
- 229920005862 polyol Polymers 0.000 description 13
- 150000003077 polyols Chemical class 0.000 description 13
- 229920001223 polyethylene glycol Polymers 0.000 description 12
- 239000000243 solution Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 238000009472 formulation Methods 0.000 description 7
- 235000006408 oxalic acid Nutrition 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 235000011187 glycerol Nutrition 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 4
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 238000007865 diluting Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000003700 vitamin C derivatives Chemical class 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 229940035437 1,3-propanediol Drugs 0.000 description 2
- 229940043375 1,5-pentanediol Drugs 0.000 description 2
- CCBICDLNWJRFPO-UHFFFAOYSA-N 2,6-dichloroindophenol Chemical compound C1=CC(O)=CC=C1N=C1C=C(Cl)C(=O)C(Cl)=C1 CCBICDLNWJRFPO-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000036074 healthy skin Effects 0.000 description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 2
- 239000008384 inner phase Substances 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000012086 standard solution Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SBJKKFFYIZUCET-JLAZNSOCSA-N Dehydro-L-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(=O)C1=O SBJKKFFYIZUCET-JLAZNSOCSA-N 0.000 description 1
- SBJKKFFYIZUCET-UHFFFAOYSA-N Dehydroascorbic acid Natural products OCC(O)C1OC(=O)C(=O)C1=O SBJKKFFYIZUCET-UHFFFAOYSA-N 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 125000003289 ascorbyl group Chemical group [H]O[C@@]([H])(C([H])([H])O*)[C@@]1([H])OC(=O)C(O*)=C1O* 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 235000020960 dehydroascorbic acid Nutrition 0.000 description 1
- 239000011615 dehydroascorbic acid Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000004770 highest occupied molecular orbital Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000008385 outer phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Abstract
The invention discloses a composition used as a cosmetic. The composition is an anhydrous system polyalcohol/silicone oil emulsion type composition containing 2-15 wt% of vitamin C based on the total weight of the composition.
Description
Technical Field
The present invention relates to the field of cosmetics. More particularly, to a cosmetic for stabilizing vitamin C.
Background
Vitamin C, as an enzyme cofactor (enzyme co-factor), can react with peroxide (superoxide) and hydroxyl radical (hydroxyl radical) when used in large quantities, and is also widely used in whitening and anti-aging products at present.
Vitamin C has a double bond structure of carbon atom No. 2 and carbon atom No. 3, and if moisture is present, oxidation reaction occurs to take away hydrogen atoms (Pk ═ 4.2), so that it has strong reducibility, and under a high pH condition, it becomes an unstable anion state, and further, it is oxidizable to dehydroascorbic acid, and it is decomposed by water. Thus, instability of vitamin C causes problems that cosmetics to which vitamin C is added are liable to suffer discoloration and a drop in titer.
In order to improve the stability problem inherent to vitamin C, a derivative of vitamin C (ascorbyl acid derivative) may be used. However, even if vitamin C derivatives are used, the loss of activity in the dosage forms is more severe because of the instability of vitamin C itself, and the skin feel is very sticky when using these dosage forms. In particular, such problems are more pronounced when high levels of vitamin C are used together with vitamin C derivatives.
Therefore, there is a strong need in the art to provide a stable cosmetic containing vitamin C.
Disclosure of Invention
The invention aims to provide a stable cosmetic containing vitamin C.
In a first aspect of the present invention, there is provided a composition for use as a cosmetic, which is a polyol/silicone oil emulsion type composition of an anhydrous system containing 2 to 15% by weight of vitamin C, based on the total weight of the composition.
In another preferred embodiment, the raw materials for preparing the composition comprise vitamin C, polyhydric alcohol, silicone oil and a silicon emulsifier; the silicone oil comprises low-viscosity silicone oil and high-viscosity silicone oil; preferably, the low viscosity silicone oil comprises polydimethylsiloxane.
In another preferred example, the content of the low-viscosity silicone oil is not less than 5 wt% based on the total weight of the raw materials.
In another preferred embodiment, the content of the silicon emulsifier is 2-10 wt% based on the total weight of the raw materials.
In another preferred embodiment, the polyol is selected from one or more of the following: POLYETHYLENE GLYCOL (POLYETHYLENE GLYCOL), POLYPROPYLENE GLYCOL (POLYPROPYLENE GLYCOL), DIPROPYLENE GLYCOL (DIPROPYLENE GLYCOL), PROPYLENE GLYCOL (PROPYLENE GLYCOL), BUTYLENE GLYCOL (BUTYLENE GLYCOL), GLYCERIN (GLYCERIN), 1, 3-PROPANEDIOL (PROPYLENE GLYCOL), and 1, 2-pentanediol (PENTYLENE GLYCOL).
In one embodiment of the present invention, the raw materials comprise, based on the total weight of the raw materials for the preparation of the composition:
in a second aspect of the present invention, there is provided a process for the preparation of a composition provided by the present invention as described above, said process comprising the steps of:
(1) mixing vitamin C and polyhydric alcohol respectively to obtain a first phase; mixing low-viscosity silicone oil, high-viscosity silicone oil and a silicon emulsifier to obtain a second phase; and
(2) the second phase is added to the first phase and intimately mixed to provide the composition of the present invention as described above.
In a third aspect of the invention, there is provided a use of a composition as provided by the invention as described above.
Accordingly, the present invention provides a stable cosmetic containing vitamin C.
Detailed Description
The inventors have conducted extensive studies and found that when vitamin C is dispersed in an anhydrous system polyol/silicone oil (P/S) formulation in its internal phase (i.e., polyol phase), the inactivation of vitamin C can be prevented by isolating the external air, moisture, heat, light, particularly, the contact with oxygen. And when the external phase (namely the silicon oil phase) is silicon oil, the phenomena of stickiness, mud rubbing and the like of vitamin C generated by absorption and evaporation of water after the skin is smeared can be improved. On the basis of this, the present invention has been completed.
As used herein, "vitamin C" refers to a compound having the structure shown in formula I:
herein, "polyol/silicone oil emulsion type (P/S emulsion type)" or "polyol/silicone oil formulation type (P/S formulation type)" both refer to a polyol-in-silicone oil emulsion system.
The polyhydric alcohol (polyol) for dispersing vitamin C provided by the invention is at least one selected from POLYETHYLENE GLYCOL (POLYETHYLENE GLYCOL), POLYPROPYLENE GLYCOL (POLYPROPYLENE GLYCOL), DIPROPYLENE GLYCOL (DIPROPYLENE GLYCOL), PROPYLENE GLYCOL (PROPYLENE GLYCOL), BUTYLENE GLYCOL (BUTYLENE GLYCOL), glycerol (glycerol), 1, 3-PROPANEDIOL (PROPYLENE GLYCOL) and 1, 2-pentanediol (PENTYLENE GLYCOL).
The silicone oil used as the external phase includes a low viscosity silicone oil having an average viscosity of 4 to 8cst (preferably 6cst) and a high viscosity silicone oil having an average viscosity of 300000cps or more.
In one embodiment of the present invention, the low viscosity silicone oil includes polydimethylsiloxane (dimethicone), and preferably cyclic polydimethylsiloxane (cyclo-methione).
In one embodiment of the present invention, the high viscosity silicone oil having an average viscosity of 300000cps or more may be Cyclomethicone, Dimethicone/Vinyl Dimethicone Crosspolymer (Cyclomethicone/Dimethicone/Vinyl Dimethicone Crosspolymer).
Silicone emulsifiers, such as PEG/PPG-18/18 polydimethylsiloxane, lauryl PEG/PPG-18/18 polymethylsiloxane, PEG/PPG-19/19 polydimethylsiloxane, bis-isobutyl PEG/PPG-10/7/polydimethylsiloxane copolymer, PEG-12 polydimethylsiloxane crosspolymer, are also necessary in the starting materials for preparing the external phase; PEG/PPG-18/18Dimethicone (PEG/PPG-18/18Dimethicone) and PEG/PPG-19/19Dimethicone (PEG/PPG-19/19Dimethicone) are preferred. The amount of the silicon emulsifier in the composition provided by the invention is not less than 2 wt% and not more than 10 wt% based on the total weight of the raw materials for obtaining the composition; when the content is less than 2.0%, the particles of the polyol/silicone oil (P/S) formulation are unstable, and when the content exceeds 10.0%, sticky feeling and slushing phenomenon occur.
The addition of vitamin C is 2.0-15.0 wt% based on the total weight of the raw materials for obtaining the composition provided by the invention; the usage amount of the polyhydric alcohol is 15-86 wt%; the usage amount of the low-viscosity silicone oil is not less than 5 wt%, and the usage amount of the high-viscosity silicone oil is 5.0-30.0 wt%; the usage amount of the silicon emulsifier is 2.0-10.0 wt%.
In one embodiment of the present invention, the composition comprises, based on the total weight of the raw materials for preparing the composition provided by the present invention, 2.0-15.0 wt% of vitamin C, 5.0-30.0 wt% of low viscosity silicone oil having an average molecular weight of 300-2000, 5.0-30.0 wt% of high viscosity silicone oil having an average molecular weight of 2000 or more, 2.0-10.0 wt% of silicon emulsifier, and the balance of polyol.
The preparation method of the composition provided by the invention comprises the following steps:
a first step of obtaining a first phase and a second phase, respectively;
and secondly, adding the second phase into the first phase, and carrying out homogeneous mixing.
The first phase in the above step is obtained by mixing vitamin C and polyhydric alcohol.
In one embodiment of the present invention, vitamin C and the polyol are mixed in the desired formula amounts and then heated to dissolve the first phase.
The second phase in the above step is the mixing of low viscosity silicone oil and high viscosity silicone oil with the silicone emulsifier.
In one embodiment of the invention, the formulated amounts of low viscosity silicone oil and high viscosity silicone oil are dispersed in the formulated amount of silicon emulsifier at ambient temperature to provide a second phase.
In one embodiment of the present invention, the first phase and the second phase obtained in the first step are thoroughly mixed using a high-speed homogenizer in the second step; preferably, the second phase is slowly added to the first phase and then the two phases are thoroughly mixed using a high speed homogenizer.
In a preferred embodiment of the present invention, the homogenizing speed is 2500-; homogenizing for 8-10 min; the emulsification temperature is 50-60 ℃; the discharging temperature is 30-35 ℃.
In a preferred embodiment of the present invention, the material thoroughly mixed in the second step is cooled and deaerated.
The composition prepared by the invention has vitamin C dispersed in an inner phase (a first phase), and silicone oil is used in an outer phase (a second phase).
The composition provided by the invention is mainly used as or used for manufacturing cosmetics, in particular cosmetics with whitening effect; the cosmetic is not limited to specific formulations, and can be developed into skin softening water, nourishing lotion, massage cream, nourishing cream, facial mask, essence, ointment, color cosmetic BASE, foundation cream, lotion, gel, cream, spray, etc.
The features mentioned above with reference to the invention, or the features mentioned with reference to the embodiments, can be combined arbitrarily. All the features disclosed in this specification may be combined in any combination, and each feature disclosed in this specification may be replaced by alternative features serving the same, equivalent or similar purpose. Thus, unless expressly stated otherwise, the features disclosed are merely generic examples of equivalent or similar features.
The main advantages of the invention are:
1. the present invention provides a cosmetic composition which can prevent the oxidation of vitamin C.
2. The cosmetic provided by the invention can avoid the direct influence of the external environment on vitamin C, increase the feeling of fit with the skin and prevent the accumulation and adhesion of the vitamin C on hands.
3. The vitamin C in the cosmetic provided by the invention is used as a solvent in the process of in vivo absorption, so that the loss of water is prevented, and a large amount of vitamin C can be more efficiently absorbed by a human body.
4. The method provided by the invention has low cost and lower requirements on equipment and process.
The invention will be further illustrated with reference to the following specific examples. It should be understood that these examples are for illustrative purposes only and are not intended to limit the scope of the present invention. The experimental procedures, in which specific conditions are not noted in the following examples, are generally carried out according to conventional conditions or according to conditions recommended by the manufacturers. All percentages, ratios, proportions, or parts are by weight unless otherwise specified. The weight volume percentage units in the present invention are well known to those skilled in the art and refer to, for example, the weight of solute in a 100 ml solution. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. In addition, any methods and materials similar or equivalent to those described herein can be used in the methods of the present invention. The preferred embodiments and materials described herein are intended to be exemplary only.
The starting materials in the examples were purchased from DOW CORING (silicone oil and silicone oil emulsifier), DSM (vitamin C), polyol (JIALI, Shell Chemicals America), respectively.
The polyol/silicone oil (P/S) emulsifiers of examples 1-4 and comparative examples 1-2 were obtained according to the raw material formulation listed in Table 1 and the following method:
manufacturing method
1) First, glycerol, propylene glycol and vitamin C are added into a beaker and heated to be dissolved.
2) The high/low viscosity silicone oil and the silicon emulsifier are completely dispersed at normal temperature.
3) The above 2 phases were slowly added to phase 1 and the two were thoroughly mixed using a high speed homogenizer (HOMO MIXER) at 6000 RPM.
4) Cooled to 33 ℃ and defoamed.
TABLE 1
Test example 1
Shape and hardness
The compositions provided in examples 1 to 4 and comparative examples 1 to 4 were stored in an incubator at 25 ℃ and then measured for hardness at various times by a Rheo meter. (Sun Rheo Meter, CR-200D, Sun Scientific Co.Ltd,(20mm),speed 120mm/min,set 20.0mm)。
the results are shown in tables 2 and 3.
TABLE 2 Change in Properties
The standard is as follows: very stable (high temperature: no delamination; low temperature: no sedimentation), stable (high temperature: degree of delamination up and down 1 mm; low temperature: fine precipitation phenomenon observed), normal (high temperature: degree of delamination up and down 5 mm; low temperature: precipitation phenomenon observed), delaminated and precipitation phenomenon observed (high temperature: separation up and down 5 mm; low temperature: severe precipitation phenomenon).
TABLE 3 hardness Change
| Categories | The day | One day | 1 week | 2 weeks | 1 month |
| Example 1 | 28 | 32 | 30 | 28 | 27 |
| Example 2 | 26 | 31 | 27 | 25 | 22 |
| Example 3 | 28 | 28 | 25 | 22 | 20 |
| Example 4 | 34 | 38 | 34 | 32 | 30 |
| Comparative example 1 | 22 | 18 | 10 | Layering | Layering |
| Comparative example 2 | 38 | 40 | 36 | 32 | 30 |
| Comparative example 3 | 21 | 13 | Layering | Layering | Layering |
| Comparative example 4 | 35 | 32 | 28 | 24 | 21 |
The results show that the examples are more excellent in stability and change in physical properties than the comparative examples. Comparative example 3 (using non-silicone oil + non-silicone oil emulsifier) showed delamination and discoloration. The types and the proportion of the silicone oil and the emulsifier selected by the invention are considered for the stability and the optimal skin feel.
Test example 2
Vitamin C titer
The titre testing method comprises the following steps:
1) 2% oxalic acid solution: dissolving 20g of oxalic acid in 700ml of distilled water, and diluting to 1000 ml;
2) 1% oxalic acid solution: taking 450ml of the 2% oxalic acid solution, and diluting to 900ml
3) Vitamin C standard solution: dissolving vitamin C20mg in 1% oxalic acid solution, adding into brown volumetric flask, adding 1% oxalic acid solution to desired volume, and shaking
4) 0.02% 2, 6-dichlorophenol indophenol solution: dissolving 52mg of sodium bicarbonate in 200ml of boiling water, weighing 49.2mg of 2, 6-dichlorophenol indophenol, dissolving in the sodium bicarbonate solution, cooling, filtering in a 250ml brown volumetric flask, diluting with water to a scale, and shaking uniformly for later use;
5) placing 2ml of 0.2mg/ml vitamin C standard solution in a triangular flask, adding 5ml of 1% oxalic acid, shaking, titrating with 0.02% prepared dye solution to reddish color, and calculating the content of vitamin C when the solution does not fade for 15s
Examples 1 to 4 and comparative examples 1 to 2 provide compositions in which the initial titer of vitamin C was 100 and the titer of vitamin C after 1 month was measured at room temperature, 37 ℃ and 40 ℃ as shown in Table 4.
TABLE 4 vitamin C titre (titer) analysis
The results show that the vitamin C titers in the compositions provided in examples 1-4 remain at high levels after 1 month of storage at room temperature. In comparative example 1, the character separation occurred in only 2 weeks, and the titer could not be measured. Comparative example 2 the titer is relatively free of major problems,
test example 3
Skin feel contrast
5 female subjects of 23 to 27 years old having healthy skin were selected, test samples (compositions provided in examples 1 to 4 and comparative examples 1 to 2) were applied to selected positions on the face of the subjects, and indices of absorption rate, sticky feeling, moisture retention, skin condition, appearance and the like were evaluated and the average value thereof was calculated.
The results are shown in Table 5.
TABLE 5
| Categories | Absorption rate | Sticky feeling | Sense of moisture retention | Rub mud with hands |
| Example 1 | 4.2 | 0.3 | 4.8 | X |
| Example 2 | 4.7 | 0.5 | 4.3 | X |
| Example 3 | 4.5 | 0.9 | 4.2 | X |
| Example 4 | 4.3 | 1.2 | 3.8 | X |
| Comparative example 1 | 4.9 | 0.7 | 2.5 | X |
| Comparative example 2 | 2.8 | 4.2 | 4.5 | 0 |
| Comparative example 3 | 3.2 | 4.6 | 2.6 | X |
| Comparative example 4 | 4.8 | 4.8 | 4.1 | X |
The results show that comparative example 2 has a sliming phenomenon and a heavy skin feel. The skin feel of comparative example 4 was heavy and the stickiness was high. The types and the proportion of the silicone oil and the emulsifier selected by the invention are considered for the stability and the optimal skin feel.
Test example 4
Test of skin whitening efficacy of human body
A23-27 year old female subject, 5 years old, with healthy skin was selected, 6 small holes 1.5cm in diameter were drawn on the arm of the subject, and the skin was blackened by irradiation with Ultraviolet (UVB) radiation at a level of 1.5-2 times the minimum Erythema Dose (minimum Erythhema Dose).
Then, the compositions provided in examples 1 to 4 and comparative examples 1 to 2 were applied 2 times per day (morning and evening), and skin complexion was measured after 2 months using a chroma meter apparatus. And calculating an L value to judge the result (the skin color value of the Chinese which is not easy to be sunburned is generally 50-70). The effect after application of the test samples is a gradual increase in the L value, and the comparison between the test samples can be found by the Δ L value (total L-value before application of the test substance). The whitening effect is more remarkable as the Δ L value is larger. Specific Δ L values can be seen in table 6.
The results are shown in Table 6.
TABLE 6
| Categories | Whitening effect (Delta L) |
| Example 1 | 3.17 |
| Example 2 | 3.12 |
| Example 3 | 3.07 |
| Example 4 | 3.20 |
| Comparative example 2 | 3.11 |
In summary, the composition provided by the invention adopts a polyol/silicone oil (P/S) formulation, a large amount of vitamin C is dispersed in the inner phase (first phase), so that the stability is increased, and the whitening effect is enhanced. And the use of silicone oil which is excellent in the external phase (second phase) in the feeling of being in contact with the skin and can bring about a soft feeling can greatly reduce the slimy feeling and the mud rub phenomenon of the product.
Therefore, the composition provided by the invention has more excellent whitening effect than other compositions, and can be applied to whitening products.
The foregoing is merely a preferred embodiment of the invention and is not intended to limit the scope of the invention, which is defined by the claims appended hereto, and any other technical entity or method that is encompassed by the claims as broadly defined herein, or equivalent variations thereof, is contemplated as being encompassed by the claims.
Claims (5)
1. A composition for use as a cosmetic, characterized in that the raw materials comprise, based on the total weight of the raw materials for the preparation of the composition:
the low viscosity silicone oil comprises polydimethylsiloxane; the high-viscosity silicone oil is a mixture of cyclomethicone, dimethicone/vinyl dimethicone crosspolymer;
the silicon emulsifier is PEG/PPG-18/18 polydimethylsiloxane and PEG/PPG-19/19 polydimethylsiloxane;
the polyhydric alcohol is glycerol and propylene glycol.
2. The composition of claim 1, wherein the low viscosity silicone oil has an average viscosity of 6 cst.
3. The composition of claim 2, wherein the high viscosity silicone oil is present in an amount of 5.0 to 15.0 wt.%.
4. A process for the preparation of a composition according to any one of claims 1 to 3, characterized in that it comprises the steps of:
(1) mixing vitamin C and polyhydric alcohol respectively to obtain a first phase; mixing low-viscosity silicone oil, high-viscosity silicone oil and a silicon emulsifier to obtain a second phase;
(2) adding the second phase to the first phase and mixing homogeneously to obtain the composition according to any one of claims 1 to 3.
5. Use of the composition according to any one of claims 1 to 3 for the manufacture of a cosmetic having whitening efficacy.
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| CN109875911A (en) * | 2019-01-31 | 2019-06-14 | 张鹭云 | An easily absorbed anhydrous nano vitamin C face cream and preparation method thereof |
| CN110101617A (en) * | 2019-05-13 | 2019-08-09 | 北京安秀植物应用技术研究有限公司 | A kind of wrinkle resistance, whitening moisturizing anhydrous formulations skin protection cosmetics and preparation method thereof |
| CN110101611B (en) * | 2019-06-21 | 2022-03-11 | 广州市澳源科技集团有限公司 | Vitamin A anhydrous emulsion and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101584647A (en) * | 2008-05-20 | 2009-11-25 | 赢创德固赛(中国)投资有限公司 | Polylol-in-oil composition with high vitamin C content and preparation method thereof |
| CN102784070A (en) * | 2011-05-16 | 2012-11-21 | 赢创德固赛特种化学(上海)有限公司 | Stable hydroquinone-containing polyol-in-oil composition and preparation method thereof |
| CN105434181A (en) * | 2015-12-30 | 2016-03-30 | 广州市科能化妆品科研有限公司 | Dual-layer water-free skin-care composition and preparation method thereof |
| CN106232100A (en) * | 2014-04-28 | 2016-12-14 | 道康宁公司 | Crosslinking composition and cosmetic composition comprising the crosslinking composition |
| CN106860051A (en) * | 2015-12-11 | 2017-06-20 | 上海家化联合股份有限公司 | One kind includes ascorbic polyalcohol bag fluid composition of high content and preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060280711A1 (en) * | 2005-06-14 | 2006-12-14 | L'oreal | Process for treating marionette lines |
-
2017
- 2017-10-24 CN CN201711002041.4A patent/CN108403473B/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101584647A (en) * | 2008-05-20 | 2009-11-25 | 赢创德固赛(中国)投资有限公司 | Polylol-in-oil composition with high vitamin C content and preparation method thereof |
| CN102784070A (en) * | 2011-05-16 | 2012-11-21 | 赢创德固赛特种化学(上海)有限公司 | Stable hydroquinone-containing polyol-in-oil composition and preparation method thereof |
| CN106232100A (en) * | 2014-04-28 | 2016-12-14 | 道康宁公司 | Crosslinking composition and cosmetic composition comprising the crosslinking composition |
| CN106860051A (en) * | 2015-12-11 | 2017-06-20 | 上海家化联合股份有限公司 | One kind includes ascorbic polyalcohol bag fluid composition of high content and preparation method thereof |
| CN105434181A (en) * | 2015-12-30 | 2016-03-30 | 广州市科能化妆品科研有限公司 | Dual-layer water-free skin-care composition and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| "用于稳定化妆品中维生素C的油包多元醇体系的研究";张海州等;《日用化学工业》;20090831;第39卷(第4期);第249-252页 * |
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